Canonical Allele Identifier: PA2580108103
Gene: CTSK HGNC NCBI

Linked Data

ClinVar Variation Id: 2481414
ClinVar RCV Id: RCV003199708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000387.1:p.Lys158Asn
CA1080506
NM_000396.4:c.474A>T
CA342336639
NM_000396.4:c.474A>C